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HCID 68494041、化合物 → N-benzyl-2-cyano-4-methylthiazole-5-carboxamide

HRID 2381778
ノート
印刷プレビュー

反応式

HRID 2381778 の反応式
[Cu][C:2]#[N:3].[CH2:4]([NH:11][C:12]([C:14]1[S:18][C:17](I)=[N:16][C:15]=1[CH3:20])=[O:13])[C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1>CN(C)C=O.O>[CH2:4]([NH:11][C:12]([C:14]1[S:18][C:17]([C:2]#[N:3])=[N:16][C:15]=1[CH3:20])=[O:13])[C:5]1[CH:6]=[CH:7][CH:8]=[CH:9][CH:10]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 68494041HCID 68494041、化合物HCID 178418546HCID 178418546、化合物

生成物 1

HCID 68492000N-benzyl-2-cyano-4-methylthiazole-5-carboxamide収率 41.6%

試薬・触媒・溶媒 2

HCID 962Water溶媒HCID 6228Dimethylformamide溶媒

実験手順

To a stirred mixture of copper(I) cyanide (0.19 g, 2.10 mmol) in anhydrous N,N-dimethylformamide (6 mL) at 150° C. was added N-benzyl-2-iodo-4-methylthiazole-5-carboxamide (0.30 g, 0.84 mmol). The resulting reaction mixture was stirred at same temperature for 10 minutes, and then allowed to cool to ambient temperature and diluted with water (50 mL). The resulting precipitate was filtered, washed with water (50 mL) and ethyl acetate (100 mL). The organic filtrate was washed with water (2×50 mL), dried over sodium sulfate, filtered and concentrated in vacuo. The residue was purified by column chromatography (0-20% ethyl acetate in hexanes) to afford the title compound as a clear oil (0.09 g, 39%): 1H NMR (300 MHz, CDCl3) δ 7.42-7.30 (m, 5H), 6.17 (br s, 1H), 4.63 (d, J=5.6 Hz, 2H), 2.73 (s, 3H); MS (ES−) m/z 256.2 (M−1).

後処理

  1. customThe resulting reaction mixture
  2. filtrationThe resulting precipitate was filtered
  3. washwashed with water (50 mL) and ethyl acetate (100 mL)
  4. washThe organic filtrate was washed with water (2×50 mL)
  5. dry with materialdried over sodium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated in vacuo
  8. customThe residue was purified by column chromatography (0-20% ethyl acetate in hexanes)

出典と根拠

ORDレコード
ord-d1533f3b925c4084a42a80b900d8332b
出典データセット
uspto-grants-2012_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08258160B2

反応ノート

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